US3139339A - Photoconductor coatings for electrophotographic purposes - Google Patents

Photoconductor coatings for electrophotographic purposes Download PDF

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US3139339A
US3139339A US67880A US6788060A US3139339A US 3139339 A US3139339 A US 3139339A US 67880 A US67880 A US 67880A US 6788060 A US6788060 A US 6788060A US 3139339 A US3139339 A US 3139339A
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formula
quinazoline
phenyl
compound
electrophotographic
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Schlesinger Heinz
Neugebauer Wilhelm
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Azoplate Corp
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Azoplate Corp
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72—Quinazolines; Hydrogenated quinazolines
    • C07D239/74—Quinazolines; Hydrogenated quinazolines with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached to ring carbon atoms of the hetero ring
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02—Charge-receiving layers
    • G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
    • G03G5/0622—Heterocyclic compounds
    • G03G5/0624—Heterocyclic compounds containing one hetero ring
    • G03G5/0635—Heterocyclic compounds containing one hetero ring being six-membered
    • G03G5/0637—Heterocyclic compounds containing one hetero ring being six-membered containing one hetero atom
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02—Charge-receiving layers
    • G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
    • G03G5/0622—Heterocyclic compounds
    • G03G5/0624—Heterocyclic compounds containing one hetero ring
    • G03G5/0635—Heterocyclic compounds containing one hetero ring being six-membered
    • G03G5/0638—Heterocyclic compounds containing one hetero ring being six-membered containing two hetero atoms

Definitions

  • Inorganic materials such as selenium and zinc oxide and various organic compounds of lower molecular weight such as anthracene and benzidine, have already been used as photoconductor coatings for electrophotographic purposes.
  • Photoconductor coatings for electrophotographic purposes consist at least in part of one or more quinazolines of the general formula in which R, is aryl or substituted aryl, R is aryl, substituted aryl, aryl-vinyl, aralkyl, aryloxy or a heterocycle and in which the aromatic ring, A, may be substituted or condensed with a ring.
  • R and R substituents which may or may not be identical, are aryl groups such as phenyl, naphthyl, phenanthryl, and anthryl; aryl-vinyl groups such as styryl; lower alkyl such as methyl, ethyl and propyl substituted by aryl (e.g., phenyl), by aryloxy (e.g., naphthoxy and phenoxy) or by heterocycles (e.g., carbazole and quinoline), and substituted aryl residues, the substituents used being those that do not essentially affect conductivity.
  • aryl groups such as phenyl, naphthyl, phenanthryl, and anthryl
  • aryl-vinyl groups such as styryl
  • lower alkyl such as methyl, ethyl and propyl substituted by aryl (e.g., phenyl), by aryloxy (e.g., naph
  • substituents are, for example, lower alkyl groups such as methyl, ethyl, propyl, butyl, and aryl; lower alkoxy groups such as methoxy ethoxy, propoxy and butoxy; nitro groups, the halogens (e.g., chlorine, bromine and iodine) amino groups, alkylated amino groups such as dimethylamino, diethylamino, dipropylamino, and acylarnino groups, e.g., acetamido groups.
  • halogens e.g., chlorine, bromine and iodine
  • alkylated amino groups such as dimethylamino, diethylamino, dipropylamino
  • acylarnino groups e.g., acetamido groups.
  • Amino groups and substituted amino groups have proved particularly advantageous. Also, a plurality of the substituents may be present in the same residue.
  • the quinazolines of the above general formulae are prepared by the condensation of N-aryl-acyl-imido chlorides or N-aryl-acyl-imino-ethers with the corresponding cyano compounds in the presence of electrophilic metal chlorides, by the synthetic method described by Meerwein et al., in Chem.-Berichte 89, 224 (1956).
  • the quinazolines described above are preferably dissolved in an organic solvent and coated upon a support, e.g., the solution is cast, painted, or sprayed thereon or applied by rollers and the solvent is then evaporated.
  • the products can also be applied in the form of aqueous or non-aqueous dispersions. Also, mixtures of the compounds may be used.
  • the quinazolines of the invention can also be used in association with resins.
  • the photoconductor coatings can thus include natural resins such as colophony, balsam resins, and shellac; synthetic resins such as colophonymodified phenol resins; other resins in which colophony is the major constituent and also coumarone resin, indene resin and compounds defined by the collective term synthetic lacquer resins.
  • cellulose ether examples include processed natural resins such as cellulose ether, polymers such as vinyl polymers, e.g., polyvinyl-chloride, polyvinylidene chloride, polyvinyl acetate, polyvinyl acetals, polyvinyl ether, and polyacrylic and polymethacrylic acid ester; also polystyrene, polyisobutylene, chlorinated rubber, and polycondensates, e.g., polyesters such as phthalate resin, alkyd resin, maleinate resins, maleic acid/colophony/mixed esters of higher alcohols; phenolformaldehyde resins, particularly colophony-modified phenol-formaldehyde condensates, urea-formaldehyde condensates, melamineformaldehyde resins, aldehyde resins, ketone resins, particularly AW2 resins, xylene-formaldehyde resins, polyarni
  • proportions of resin to photoconductor material can vary very greatly. Proportions of between two parts of resin to one part of photoconductor material and two parts of photoconductor material to one part of resin are preferable. Mixtures of the two materials in equal proportions by weight are particularly favorable. However, where resins are used in the coatings, the content of photoconductive compound should be at least 20 percent.
  • the base materials used as supports may be any that satisfy the requirements of electrophotography, e.g., metal or glass plates, paper or plates or foils made of electroconductive resins or plastics, such as polyvinyl alcohol, polyamides, and polyurethanes.
  • electroconductive resins or plastics such as polyvinyl alcohol, polyamides, and polyurethanes.
  • Other plastics which have the required electroconductivity such as cellulose acetate and cellulose butyrate, especially in a partially saponified form, polyesters, polycarbonates, and polyolefines, if they are covered with an electroconductive layer or if they are converted into electroconductive materials, e.g., by chemical treatment with or by introduction of materials which render them electrically conductive, may also be used.
  • electroconductive supports are suitable for the purposes of the present invention.
  • the term electroconductive support comprises materials having a specific conductivity higher than 10- ohmfhcmr preferably higher than 10* ohm .cm.
  • the supporting material provided with a thin coherent coating of even thickness of the photoconductor layer as described above, is used for the preparation of copies by electrophotographic means in the following manner:
  • the photoconductor coating is evenly charged in the absence of light, e.g., by a corona discharge from a charging device maintained at 6000-7000 volts.
  • the electrocopying material is then exposed to light under a master or, alternatively, an episcopic or diascopic image of the master is projected thereon.
  • An electrostatic image corresponding to the master is then formed on the material. This invisible image is developed by contact with a developer consisting of a carrier and a toner.
  • the toner consists of a mixture of resin and carbon black or of pigmented resin.
  • the toner is generally used in a particle size of about 1-10Qu preferably 530,u.
  • the developer may also consist of a resin or pigment suspended in a dielectric liquid in which resins may be dissolved.
  • the image which has been rendered visible is then fixed, e.g., by heating to 100-170 C., preferably 120-150 C., with an infra-red radiator, or by treatment with solvents such as trichloroethylene, carbon tetrachloride, ethyl alcohol or steam. In this manner images are obtained which correspond to the masters and which have good contrast effect.
  • electrophotographic images can also be converted into printing plates.
  • they are wiped'over with asuitable solvent, or with a preferably alkaline aqueous developer liquid, rinsed down with' water and then inked up with greasy ink.
  • printing plates are obtained which can be set up in an offset machine and used for printing.
  • the electrophotographic images can also be used as masters for further copying on any type of coatings.
  • images can also be produced by the reflex process.
  • Sensitizers can be added to the photoconductor coatings to increase the sensitivity thereof. Such sensitizers are effective even in very small quantities, e.g., less than 0.01 percent. In general, however, 0.01 to 5 percent, preferably 0.05 to 3 percent of dyestutf sensitizer is added to the photoconductor coatings. The addition of larger quantities is possible but in general is not accompanied by any significant increase in sensitivity.
  • dyestufi sensitizers which may be used with good results, and some with very good results. They are taken from Schultz Farbstofltabellen, 7th edition, 1931, 1st vol.:
  • Triarylmethane dyestuffs such as Brilliant Green (No. 760, p. 314), Victoria'Blue B (No. 822, p. 347), Methyl Violet.(No. 783, p. 327), Crystal Violet (No. 785, p. 329), Acid Violet 6B (No. 831, p. 351); xanthene dyestuffs, namely rhod-amines, such as Rhodamine B (No. 864, p. 365), Rhodamine 6G (No. 866, p. 366), Sulphorhodamine B (No. 863, p. 364) and Fast Acid Eosin G (No. 870, p.
  • Eosin S No. 883, p. 375
  • Eosin A No. 881, p. 374
  • Erythrosin No. 886, p. 376
  • Phloxin No. 890, p. 378
  • Bengal Rose No. 889, p. 378
  • Fluorescein No. 880, p. 373
  • thiazine dyestuffs such as Methylene Blue (No. 1038, p. 449)
  • acridine dyestuffs such as Acridine Yellow (No. 901, p. 383), Acridine Orange (No. 908, p. 387) and Trypafiavine (No. 906, p.
  • quinoline dyestuffs such as Pinacyanol (No. 924, p. 396) and Cryptocyanine (No. 927, p. 3 97); cyanine dyestuffs, e.g., Cyanine (No. 921, p. 394) and chlorophyll.
  • photoconductor coatings described above can be used both in reproduction processes and in measuring instruments for recording purposes, e.g., photographic recording instruments. They can also be used in the production of other devices containing photoconductors, e.g., photoelectric cells, photoresistances, sensing heads or camera tubes.
  • the photoconductor coatings of the present invention may also be used in association with other photoconductors and with pigments such as titanium dioxide.
  • 2-phenyl-4-(4'- dimethyl aminophenyl) quinazoline corresponding to Compound 3 of the table, is prepared as follows: 6.7 parts by weight of powdered anhydrous aluminum chloride are added to a solution of 10.3 parts by weight of benzanilide imidochloride and 7.3 parts by weight of 4-dimethylamino-benzonitrile in 100 parts by volume of dry 1,2-dichlorobenzene at C. and the mixture is stirred for two hours at this temperature.
  • coating is provided with a negative electric charge using a corona discharge produced from a charging apparatus maintained at about 6000 volts, exposed beneath toluene, a firmly adherent coating remains.
  • a master to the light of a high-pressure mercury vapor lamp (125 watts) and then dusted over with a developer in known manner.
  • the developer consists of tiny glass balls and a very finely dividedresin/carbon black mixture known as the toner.
  • the black colored resin adheres to those portions that were not affected by the light during the exposure and an image corresponding to the master becomes visible. It is fixed by heating.
  • the developer used in the above case consists of 100 parts by weight of glass balls of a particle size of 350- 400,0. and 2.5 parts by weight of a toner of a particle size of 20-5 O
  • the toner is obtained by melting together 30 parts by weight of polystyrene, 30 parts by Weight of a modified maleic acid resin (e.g., Beckacite K105) and 3 parts by weight of carbon black (e.g., Peerless Black Russ 552), after which the melt is ground and screened.
  • a modified maleic acid resin e.g., Beckacite K105
  • carbon black e.g., Peerless Black Russ 552
  • Example 2 Paper is coated, as described in Example 1, and the coating is provided, by a corona discharge, with a positive charge. After it has been exposed to light under a master, the image thus produced on a paper foil is developed by dusting over with a developer, as described in Example 1, but with glass balls covered with resin, e.g., coumarone resin, as a carrier. As the coumarone resin coating for the glass balls, the commercial product Cumaronharz 601/90 is advantageously used. A good positive image of the master, rich in contrast, is similarly obtained.
  • resin e.g., coumarone resin
  • Example 3 0.5 part by weight of 2-phenyl-4-(4K-dimethylaminophenyl)-quinazoline (Compound 3 of the table) and 0.5 part by weight of an unsaponified ketone-aldehyde condensation resin (Kunstharz AP) are dissolved in 15 parts by volume of ethyleneglycol monomethylether. The solution is applied to an aluminum foil. After the solvent has evaporated, a coating remains which adheres firmly to the surface of the foil. With the coated aluminum foil, images can be prepared from masters electrophotographically in a manner known per se.
  • Example 4 0.17 part by weight of each of the following three quinazolines are dissolved in 15 parts by volume of toluene:
  • Example 5 0.5 part by weight of 2-phenyl-4-anthranyl-(9')-quinazoline (Compound 6 of the table) and 0.5 part by weight of a ketone resin (Kunstharz SK) are dissolved in 15 parts by volume of toluene. The solution is coated on an aluminum foil, upon which, after evaporation of the Electrophotographic images are prepared as described in Example 1.
  • Example 6 0.5 part by weight of 2-phenyl-4-(4-dimethylaminophenyl)-quinazoline (Compound 3 of the table), 0.5 part by weight of a ketone resin (Kunstharz SK) and 0.005 part by weight of Ethyl Violet (Schultz Farbstotftabellen, 7th edition, vol. I, No. 787) are dissolved in 15 parts by volume of ethyleneglycol monomethylether.
  • the solution is coated upon paper. After it has dried, an electrophotographic image is prepared, as described in Example 1, a IOO-Watt filament lamp being used for the exposure.
  • Example 7 0.5 .part by weight of a chlorinated polyvinyl chloride (Rhenoflex) is dissolved in 5 parts by volume of methyl-ethyl-ketone and 0.5 part by Weight of 2,4-diphenyl- 7,8-benzo-quinazoline (Compound 19 of the table), dissolved in 10 parts by volume of toluene, is added to this solution. The solution is then coated upon a transparent paper lacquered With acetyl cellulose. Images are then produced on this transparent paper by the electrophotographic process. They can be used as intermediate originals for further copying, on diazo paper, for example.
  • Rhoflex chlorinated polyvinyl chloride
  • Compound 19 of the table 2,4-diphenyl- 7,8-benzo-quinazoline
  • An electrophotographic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a quinazoline compound having the formula in which R and R arearyl groups.
  • An electrophotographic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a quinazoline compound having the formula in which R is an aryl and R is alkyl group.
  • An electrophotographic material comprising a conductive support layer and a photoconductive insulating l. 1 layer, the latter comprising a quinazoline compound having the formula 6.
  • An electrophotographic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a quinazoline compound having the formula 7.
  • An electrophotographic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a quinazoline compound having the formula 8.
  • An electrophotographic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a quinazoline compound having the formula L ⁇ N/ Q l in which R is an ortho-arylene group, R is an aryl group, and R is selected from the group consisting of aryl, alkyl, aralkylene, and aralkyl groups.
  • the pho-t toconductive layer contains at least one compound se- 'lected from the group consisting of resins and optical sensitizers.
  • a photographic reproduction process which comprises exposing an electrostatically charged supported photoconductive insulating layer to light under a master and developing theresultingiimage .with an electroscopic material, the photoconductive layer comprising a quinazoline compound having the formula in which R is an aryl and R is an alkyl group.
  • a photographic reproduction process which comprises exposing an electrostatically charged supported photoconductive insulating layer'to light under a master and developing the resulting image with. an electroscopic material, the photoconductive layer comprising a quinazoline compound having the formula 14.
  • a photographic reproduction process which comprises exposing an electrostatically charged supported photoconductive insulating layer to light under a master and developing the resulting image with an electroscopic material, the photoconductive layer comprising a quinazoline compound having the formula photoconductive insulating layer to light under a master and developing the resulting image with an electroscopic material, the photoconductive layer comprising a quinazoline compound having the formula 16.
  • a photographic reproduction process which comprises exposing an electrostatically charged supported photoconductive insulating layer to light under a master and developing the resulting image with an electroscopic material, the photoconductive layer comprising a quinazoline compound having the formula 17.
  • An electrophotographic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a quinazoline compound having the formula HECPN C 1H5 18.
  • a photographic reproduction process which comprises exposing a charged supported photoconductive insulating layer to light under a master and developing the resulting image, the photoconductive layer comprising a quinazoline compound having the formula 19.
  • An electrophotographic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a quinazoline compound having the formula 20.
  • An electrophotographic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a quinazoline compound having the formula 21.
  • An electrophotographic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a quinazoline compound having the formula 22.
  • An electrophotographic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a quinazoline com 7 pound having the formula, V Y
  • An electrophotographic material comprising a conductive support layer and a photoconductive insulating layer, the latter comprising a quinazoline compound having the formula 24.
  • a photographic reproduction process which comprises exposing an electrostatically supported photoconductive insulating layer to light under a master and developing the resulting image with an electroscopic material, the photoconductive layer comprising a quinazoline compound having the formula CHr-CHr-N 27.
  • a photographic reproduction process which comprises exposing an electrostatically charged supported photoconductive insulating layer to light under a master and developing the resulting image with an electroscopic material, the photoconductive layer comprising a quinazoline compound having the formula 28.
  • a photographic reproduction process which comprises exposing an electrostatically charged supported photoconductive insulating layer to light under a master and developing the resultingimage with an electroscopic material, the photoconductive layer comprising a quinazoline compound having the formula References Cited in the file of this patent UNITED STATES PATENTS 1,780,879 Hentrich et a1. Nov. 4, 1930 2,176,413 Baumann et a1. Oct. 17, 1939 2,954,291 Clark Sept. 27, 1960 FOREIGN PATENTS 562,336 Belgium n May 13, 1958 1,074,047 Germany Jan. 28, 1960 OTHER REFERENCES Vartanian: Acta Physicochimica URSS 22, pp. 201-24 (1947), 96-1PC.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Photoreceptors In Electrophotography (AREA)
US67880A 1959-11-26 1960-11-08 Photoconductor coatings for electrophotographic purposes Expired - Lifetime US3139339A (en)

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Application Number Priority Date Filing Date Title
DEK39267A DE1175076B (de) 1959-11-26 1959-11-26 Photoleiterschichten, insbesondere fuer elektrophotographische Zwecke

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108752282A (zh) * 2018-03-12 2018-11-06 温州大学 一种稠杂环医药中间体的合成方法

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6184226B1 (en) * 1998-08-28 2001-02-06 Scios Inc. Quinazoline derivatives as inhibitors of P-38 α

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE562336A (en)) * 1956-11-14
US1780879A (en) * 1930-11-04 Winerid hentrich and max hardtmann
US2176413A (en) * 1937-04-16 1939-10-17 Gen Aniline Works Inc 1.3-diaza-anthraquinones
DE1074047B (de) * 1960-01-28 Schering Aktiengesellschaft, Berlin Verfahren zur Herstellung von Chinazolmen
US2954291A (en) * 1957-01-04 1960-09-27 Haloid Xerox Inc Method for preparing a spirit duplicating master

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1780879A (en) * 1930-11-04 Winerid hentrich and max hardtmann
DE1074047B (de) * 1960-01-28 Schering Aktiengesellschaft, Berlin Verfahren zur Herstellung von Chinazolmen
US2176413A (en) * 1937-04-16 1939-10-17 Gen Aniline Works Inc 1.3-diaza-anthraquinones
BE562336A (en)) * 1956-11-14
US2954291A (en) * 1957-01-04 1960-09-27 Haloid Xerox Inc Method for preparing a spirit duplicating master

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108752282A (zh) * 2018-03-12 2018-11-06 温州大学 一种稠杂环医药中间体的合成方法
CN108752282B (zh) * 2018-03-12 2020-06-30 温州大学 一种稠杂环医药中间体的合成方法

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